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Angiotensin‐converting enzyme 2 antagonizes angiotensin II‐induced pressor response and NADPH oxidase activation in Wistar–Kyoto rats and spontaneously hypertensive rats
Author(s) -
Lo Jennifer,
Patel Vaibhav B.,
Wang Zuocheng,
Levasseur Jody,
Kaufman Susan,
Penninger Josef M.,
Oudit Gavin Y.
Publication year - 2013
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/expphysiol.2012.067165
Subject(s) - angiotensin ii , nadph oxidase , medicine , endocrinology , renin–angiotensin system , superoxide , angiotensin converting enzyme 2 , chemistry , kidney , angiotensin converting enzyme , angiotensin ii receptor type 1 , blood pressure , oxidative stress , enzyme , biochemistry , disease , covid-19 , infectious disease (medical specialty)
New Findings• What is the central question of this study? Angiotensin‐converting enzyme 2 (ACE2), an enzyme which converts angiotensin II (Ang II) into angiotensin‐(1–7) [Ang‐(1–7)] and terminates the effects of Ang II, is a negative regulator of activated renin‐angiotensin system (RAS). Cardiac overexpression of ACE2 has shown conflicting results on myocardial fibrosis in contrast to marked anti‐ hypertensive and anti‐remodelling properties. • What is the main finding and its importance? Recombinant hACE2 administration attenuates oxidative stress, NADPH oxidase activity and ERK1/2 signalling and high blood pressure confirming its beneficial role in two rat models of hypertension.Angiotensin‐converting enzyme 2 (ACE2), a monocarboxypeptidase capable of metabolizing angiotensin II (Ang II) into angiotensin‐(1–7) [Ang‐(1–7)], has emerged as a potential therapeutic target. We hypothesized that ACE2 is a negative regulator of Ang II‐mediated pathological effects in vivo . In Wistar–Kyoto (WKY) rats, Ang II infusion (0.1 μg min −1 kg −1 ) induced a pressor response, activation of NADPH oxidase and generation of superoxide in the heart, kidney and blood vessels; these effects were significantly blunted by recombinant human ACE2 (rhACE2; 2 mg kg −1 ), in association with a lowering of plasma Ang II and elevation of Ang‐(1–7) levels. In the spontaneously hypertensive rat (SHR) model, rhACE2 (2 mg kg −1 day −1 ) delivered over a 14 day period partly corrected the hypertension, the NADPH oxidase activation and the increased superoxide generation in the heart, kidney and blood vessels. Treatment with rhACE2 inhibited Ang II‐mediated phosphorylation of the myocardial extracellular signal‐regulated kinase 1/2 pathway in WKY rats, with congruent results seen in SHR hearts. Hence, rhACE2 is an important negative regulator of the Ang II‐induced pressor response and NADPH oxidase activation and suppresses pathological myocardial signalling, thereby providing a novel therapeutic agent with which to antagonize an activated renin–angiotesin system.